Medison Pharma is a global pharmaceutical company that helps bring innovative therapies to patients in international markets. Its international commercialization platform supports the launch and availability of novel treatments across territories, while partnerships with pharmaceutical and biotechnology companies help extend the reach of medicines and improve access for patients worldwide.
Regulatory Affairs Specialist – Israel (Hybrid)
Prepare and maintain pharmaceutical product registrations, renewals, variations, patient leaflets, and packaging. Coordinate regulatory work with Israel’s Ministry of Health and international partners.
Description
- Compile registration dossiers and verify that their contents meet applicable requirements
- Write consumer leaflets
- Develop product packaging
- Manage regulatory changes, renewals, updates, and leaflet requirements
- Support activities across the pharmacy division
- Prepare submissions for products, renewals, variations, leaflets, and packaging
- Keep product regulatory dossiers current
- Liaise directly with Israel’s Ministry of Health and partners abroad
- Review regulatory materials and documents
Requirements
- Bachelor’s degree in pharmacy or a life science field such as chemistry or biology
- At least two years of Israeli regulatory affairs experience, including pharmaceutical product registrations, renewals, and variations
- Strong English skills
- Excellent Hebrew skills
- Proficiency with Microsoft Outlook, PowerPoint, Word, and Excel
- Strong attention to detail
- Ability to work under pressure
- Energetic and hardworking approach
- Trustworthy conduct